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青年复发性川崎病伴草莓舌和皮肤脱皮。

Recurrent Kawasaki disease with strawberry tongue and skin desquamation in a young adult.

机构信息

Division of Rheumatology, Department of Medicine, Johns Hopkins Hospital, Baltimore, MD 21224, USA.

出版信息

J Clin Rheumatol. 2012 Mar;18(2):96-8. doi: 10.1097/RHU.0b013e31823e6b6d.

Abstract

A 19-year-old man with history of Kawasaki disease (KD) at age 12 developed intractable fevers, swelling in hands and feet, arthralgias, and conjunctivitis, followed by strawberry tongue and desquamation of distal extremities. Laboratory studies revealed leukocytosis, thrombocytosis, anemia, elevated erythrocyte sedimentation rate and C-reactive protein levels, and mildly elevated liver enzymes. He was empirically treated with broad-spectrum antibiotics without any improvement. Extensive infectious and rheumatologic workup remained negative. Recurrence of KD was diagnosed based on characteristic mucocutaneous changes and systemic inflammatory response. His symptoms and laboratory values responded rapidly to intravenous immunoglobulin and aspirin therapy. An echocardiogram did not show any coronary abnormality. We report the third case of pediatric KD relapsing in adulthood. Similar to childhood and adult KD, these recurrent episodes respond well to intravenous immunoglobulin therapy. Although recurrent KD is rare, our case highlights the importance of considering it in the differential of febrile illness in the appropriate individual.

摘要

一名 19 岁男性,12 岁时曾患川崎病(KD),出现高热、手足肿胀、关节痛和结膜炎,继之出现草莓舌和四肢远端脱皮。实验室检查显示白细胞增多、血小板增多、贫血、红细胞沉降率和 C 反应蛋白水平升高,以及肝酶轻度升高。他曾接受经验性广谱抗生素治疗,但无任何改善。广泛的感染和风湿性疾病检查仍为阴性。根据特征性黏膜皮肤变化和全身炎症反应,诊断为 KD 复发。他的症状和实验室值对静脉注射免疫球蛋白和阿司匹林治疗迅速反应。超声心动图未显示任何冠状动脉异常。我们报告了第三例儿童 KD 复发至成年。与儿童和成人 KD 相似,这些复发性发作对静脉注射免疫球蛋白治疗反应良好。虽然复发性 KD 很少见,但我们的病例强调了在适当的个体中,将其作为发热性疾病的鉴别诊断的重要性。

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